Evidence map›Paper›PMID 40853479›Full record

ArticleHuman genetics2025

uAUG-creating variant in the LDLR gene causes mild Familial hypercholesterolemia.

Alexandra Filatova, Petr Vasiluev, Evgeniya Osipova, Olga Ivanova, Natalia Semenova, Mikhail Skoblov

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Article in Human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Alexandra FilatovaResearch Centre for Medical Genetics, Moscow, Russia.ORCID http://orcid.org/0000-0002-5979-0727
Petr VasiluevResearch Centre for Medical Genetics, Moscow, Russia.ORCID http://orcid.org/0000-0002-8249-343X
Evgeniya OsipovaResearch Centre for Medical Genetics, Moscow, Russia.ORCID http://orcid.org/0009-0004-9238-2356
Olga IvanovaResearch Centre for Medical Genetics, Moscow, Russia.ORCID http://orcid.org/0000-0002-8366-2004
Natalia SemenovaResearch Centre for Medical Genetics, Moscow, Russia.
Mikhail SkoblovResearch Centre for Medical Genetics, Moscow, Russia. mskoblov@gmail.com.ORCID http://orcid.org/0000-0002-7293-3438

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial hypercholesterolemia (FH) is a genetic disorder characterized by elevated low-density lipoprotein (LDL) levels, leading to early-onset cardiovascular disease. FH is primarily caused by pathogenic variants in the LDLR gene, affecting cholesterol metabolism. We describe a family with a mild form of FH, in which gene panel sequencing identified a novel c.-8C>A variant in the LDLR 5'UTR. To assess its functional impact, we performed a luciferase assay and found that this variant partially reduces LDLR protein translation efficiency by introducing a novel upstream AUG (uAUG) start codon. This partial reduction in LDLR activity is consistent with the mild phenotype observed in the family. Additionally, we analyzed three previously reported LDLR 5'UTR variants (c.-5C>T, c.-14C>A, and c.-23A>C) but did not observe any significant effect on LDLR expression, suggesting that these variants are unlikely to contribute to disease development. These findings highlight the role of 5'UTR variants in LDLR expression and emphasize the importance of functional studies in variant classification for FH diagnostics.

Indexed as

Hyperlipoproteinemia Type IIReceptors, LDL5' Untranslated RegionsAdultCodon, InitiatorFemaleHumansMaleMiddle AgedMutationPedigree5' Untranslated RegionsCodon, InitiatorLDLR protein, humanReceptors, LDL

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.